Draw the structure of the compound whose spectroscopy data is provided. C,H120 2.6 ppm, 1H, sextet 2.1 ppm, 3H, singlet 1.7 - 1.3 ppm, 2H, multiplet 1.1 ppm, 3H, doublet 0.9 ppm, 3H, triplet
Analyzing Infrared Spectra
The electromagnetic radiation or frequency is classified into radio-waves, micro-waves, infrared, visible, ultraviolet, X-rays and gamma rays. The infrared spectra emission refers to the portion between the visible and the microwave areas of electromagnetic spectrum. This spectral area is usually divided into three parts, near infrared (14,290 – 4000 cm-1), mid infrared (4000 – 400 cm-1), and far infrared (700 – 200 cm-1), respectively. The number set is the number of the wave (cm-1).
IR Spectrum Of Cyclohexanone
It is the analysis of the structure of cyclohexaone using IR data interpretation.
IR Spectrum Of Anisole
Interpretation of anisole using IR spectrum obtained from IR analysis.
IR Spectroscopy
Infrared (IR) or vibrational spectroscopy is a method used for analyzing the particle's vibratory transformations. This is one of the very popular spectroscopic approaches employed by inorganic as well as organic laboratories because it is helpful in evaluating and distinguishing the frameworks of the molecules. The infra-red spectroscopy process or procedure is carried out using a tool called an infrared spectrometer to obtain an infrared spectral (or spectrophotometer).
![**Title: Analyzing Spectroscopy Data of a Compound**
**Objective:**
Draw the structure of the compound using the given spectroscopy data.
**Compound Formula:**
\[ \text{C}_6\text{H}_{12}\text{O} \]
**Spectroscopy Data:**
- **2.6 ppm, 1H, sextet:** Indicates a hydrogen atom experiencing coupling with five neighboring hydrogen atoms.
- **2.1 ppm, 3H, singlet:** Suggests a group of three hydrogen atoms in a chemical environment without neighboring hydrogens causing splitting.
- **1.7 – 1.3 ppm, 2H, multiplet:** Represents two hydrogen atoms experiencing a complex coupling pattern with nearby hydrogens.
- **1.1 ppm, 3H, doublet:** Indicates three hydrogen atoms next to a single neighboring hydrogen atom causing splitting.
- **0.9 ppm, 3H, triplet:** Reflects a set of three hydrogen atoms coupled with two equivalent neighboring hydrogen atoms.
**Discussion:**
Considerations for drawing the structure include analyzing the chemical shifts and multiplicity in connection with known splitting patterns, typical of various structural environments in organic molecules.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Feb95f2b3-fba9-4070-9e8f-e2a612501e51%2F4d308a42-50ac-40f4-b18f-52a8eb63ba39%2Ffe7o3n9_processed.jpeg&w=3840&q=75)
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